Die Postoperative Kontinuierliche Peritonealspülung Mit Ringer-Lactat-Lösung Zur Prophylaxe Des Adhäsionsrezidivs Nach Laparoskopischer Adhäsiolyse

Total Page:16

File Type:pdf, Size:1020Kb

Die Postoperative Kontinuierliche Peritonealspülung Mit Ringer-Lactat-Lösung Zur Prophylaxe Des Adhäsionsrezidivs Nach Laparoskopischer Adhäsiolyse Aus der Klinik und Poliklinik für Frauenheilkunde und Geburtshilfe (Direktor/in Univ.-Prof. Dr. med. Dr. hc. Wolfgang Straube) der Medizinischen Fakultät der Ernst-Moritz-Arndt-Universität Greifswald und der Abteilung für Gynäkologie (Teamchef PD Dr. med. habil. B. Bojahr) der Klinik für Minimal Invasive Chirurgie in Berlin Die postoperative kontinuierliche Peritonealspülung mit Ringer-Lactat-Lösung zur Prophylaxe des Adhäsionsrezidivs nach laparoskopischer Adhäsiolyse Eine retrospektive Untersuchung Inaugural-Dissertation zur Erlangung des akademischen Grades Doktor der Medizin (Dr. med.) der Medizinischen Fakultät der Ernst-Moritz-Arndt-Universität Greifswald, 2005 vorgelegt von: Martin Gerhard Wilhelm Hänel geb. am: 20. September 1971 in: Marburg an der Lahn i Dekan: Prof. Dr. rer. nat. Heyo K. Kroemer 1. Gutachter: 2. Gutachter: 3. Gutachter: Ort, Raum: Tag der Disputation: ii Inhaltsverzeichnis 1 Einleitung..................................................................................................................... 1 1.1 Adhäsionen und ihre Bedeutung............................................................................ 1 1.2 Pathogenese peritonealer Adhäsionen.................................................................. 1 1.2.1 Heilung von Peritonealdefekten........................................................................... 1 1.2.2 Entstehung von Adhäsionen................................................................................ 2 1.2.3 Ursachen von Adhäsionen................................................................................... 3 1.2.3.1 Kongenitale Verwachsungen........................................................................ 3 1.2.3.2 Operationen im Bereich der Bauchhöhle...................................................... 3 1.2.3.3 Fremdkörperreaktion..................................................................................... 4 1.2.3.4 Infektionen.................................................................................................... 4 1.2.3.5 Endometriose................................................................................................ 5 1.2.3.6 Ischämie........................................................................................................ 5 1.2.3.7 Blutung.......................................................................................................... 5 1.3 Klassifikation von Adhäsionen............................................................................... 5 1.4 Prävalenz von Adhäsionen...................................................................................... 5 1.5 Folgen von Adhäsionen........................................................................................... 6 1.5.1 Gesundheitliche Folgen....................................................................................... 6 1.5.1.1 Schmerzen.................................................................................................... 6 1.5.1.2 Ileus.............................................................................................................. 6 1.5.1.3 Sterilität der Frau........................................................................................... 7 1.5.1.4 Komplikationen bei Folgeeingriffen............................................................... 7 1.5.2 Wirtschaftliche Aspekte....................................................................................... 7 1.6 Möglichkeiten der Therapie von Adhäsionen........................................................ 8 1.7 Möglichkeiten der Prophylaxe von Adhäsionen.................................................... 9 1.7.1 Allgemeine Maßnahmen...................................................................................... 9 1.7.2 Adjuvante medikamentöse Maßnahmen............................................................. 9 1.7.2.1 Systemische Prophylaxe............................................................................... 9 1.7.2.2 Topische Prophylaxe................................................................................... 12 iii 1.7.2.2.1 Flüssige Barrieren................................................................................ 12 1.7.2.2.2 Feste Barrieren..................................................................................... 15 1.7.2.2.3 Lavage mit Zusatzstoffen/topische Wirkstoffe...................................... 16 1.8 Adhäsionen, Adhäsiolyse, Schmerzen und Adhäsionsprophylaxe...................18 1.9 Fragestellung.......................................................................................................... 19 2 Material und Methode............................................................................................... 21 2.1 Material.................................................................................................................... 21 2.2 Methode.................................................................................................................. 23 2.2.1 Adhäsiolyse und Vorbereitung zur Spülung....................................................... 23 2.2.2 Spülung............................................................................................................. 24 2.2.2.1 Postoperative Klarspülung.......................................................................... 24 2.2.2.2 Adhäsionsspülung....................................................................................... 24 2.2.2.3 Klar-/Adhäsionsspülung.............................................................................. 25 2.2.2.4 Septische Massivspülung............................................................................ 25 2.2.3 Auswahl des Patientenguts............................................................................... 25 2.2.3.1 Einschlusskriterien...................................................................................... 25 2.2.3.2 Ausschlusskriterien..................................................................................... 26 2.2.3.3 Selektion des Datenmaterials..................................................................... 26 2.2.3.4 Detailsuche................................................................................................. 28 2.2.3.5 Aufteilung in die Kollektive „mit Spülung“ und „ohne Spülung“....................28 2.2.4 Spülarten, Spüldauer und Anzahl der Spüldrains.............................................. 29 2.2.5 Objektivierung der Adhäsionen.......................................................................... 29 2.2.6 Objektivierung des intraoperativen Adhäsiolyseerfolges................................... 32 2.2.7 Objektivierung des Adhäsionsrezidivs............................................................... 32 2.2.8 Objektivierung des tatsächlichen Adhäsiolyseerfolges...................................... 33 2.2.9 Beobachtungen zum Schmerzempfinden.......................................................... 33 2.2.10 Beobachtungen zu Operationsindikationen und Diagnosen............................ 34 2.2.11 Beobachtungen zu den einzelnen Operateuren.............................................. 34 2.2.12 Beobachtung zum zeitlichen Verhalten von Adhäsionen................................. 34 2.3 Verwendete Software............................................................................................. 35 iv 2.4 Statistische Tests................................................................................................... 35 3 Ergebnisse................................................................................................................. 36 3.1 Ergebnisse des Auswahlprozesses..................................................................... 36 3.2 Altersverteilung der Kollektive............................................................................. 37 3.3 Zeitabstände zwischen den beiden Operationen................................................ 38 3.4 Dauer der Operationen.......................................................................................... 39 3.5 Patientinnen mit Voroperationen bei der ersten Operation............................... 40 3.6 Indikationen und Diagnosen der ersten Operation............................................. 40 3.7 Schmerzen.............................................................................................................. 45 3.8 Auswertung der Spülarten, Spüldauer und verwendeten Drains...................... 46 3.9 Auswertung der laparoskopischen Adhäsiolyse................................................ 50 3.9.1 Adhäsionsscore präoperativ.............................................................................. 50 3.9.2 Indikationsabhängiger Adhäsionsscore............................................................. 53 3.9.3 Adhäsionsscoreverlauf...................................................................................... 55 3.9.4 Effekt der Adhäsiolyse auf den Adhäsionsscore................................................57 3.10 Adhäsionsrezidiv.................................................................................................. 58 3.11 Tatsächlicher Adhäsiolyseerfolg........................................................................ 59 3.12 Indikationsabhängiger Adhäsiolyseerfolg......................................................... 61 3.13 Erfolg der Adhäsiolyse in Abhängigkeit vom Operateur.................................. 62 3.14 Untersuchung zum zeitlichen Verhalten von Adhäsionen..............................
Recommended publications
  • (12) Patent Application Publication (10) Pub. No.: US 2006/0110428A1 De Juan Et Al
    US 200601 10428A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2006/0110428A1 de Juan et al. (43) Pub. Date: May 25, 2006 (54) METHODS AND DEVICES FOR THE Publication Classification TREATMENT OF OCULAR CONDITIONS (51) Int. Cl. (76) Inventors: Eugene de Juan, LaCanada, CA (US); A6F 2/00 (2006.01) Signe E. Varner, Los Angeles, CA (52) U.S. Cl. .............................................................. 424/427 (US); Laurie R. Lawin, New Brighton, MN (US) (57) ABSTRACT Correspondence Address: Featured is a method for instilling one or more bioactive SCOTT PRIBNOW agents into ocular tissue within an eye of a patient for the Kagan Binder, PLLC treatment of an ocular condition, the method comprising Suite 200 concurrently using at least two of the following bioactive 221 Main Street North agent delivery methods (A)-(C): Stillwater, MN 55082 (US) (A) implanting a Sustained release delivery device com (21) Appl. No.: 11/175,850 prising one or more bioactive agents in a posterior region of the eye so that it delivers the one or more (22) Filed: Jul. 5, 2005 bioactive agents into the vitreous humor of the eye; (B) instilling (e.g., injecting or implanting) one or more Related U.S. Application Data bioactive agents Subretinally; and (60) Provisional application No. 60/585,236, filed on Jul. (C) instilling (e.g., injecting or delivering by ocular ion 2, 2004. Provisional application No. 60/669,701, filed tophoresis) one or more bioactive agents into the Vit on Apr. 8, 2005. reous humor of the eye. Patent Application Publication May 25, 2006 Sheet 1 of 22 US 2006/0110428A1 R 2 2 C.6 Fig.
    [Show full text]
  • Tanibirumab (CUI C3490677) Add to Cart
    5/17/2018 NCI Metathesaurus Contains Exact Match Begins With Name Code Property Relationship Source ALL Advanced Search NCIm Version: 201706 Version 2.8 (using LexEVS 6.5) Home | NCIt Hierarchy | Sources | Help Suggest changes to this concept Tanibirumab (CUI C3490677) Add to Cart Table of Contents Terms & Properties Synonym Details Relationships By Source Terms & Properties Concept Unique Identifier (CUI): C3490677 NCI Thesaurus Code: C102877 (see NCI Thesaurus info) Semantic Type: Immunologic Factor Semantic Type: Amino Acid, Peptide, or Protein Semantic Type: Pharmacologic Substance NCIt Definition: A fully human monoclonal antibody targeting the vascular endothelial growth factor receptor 2 (VEGFR2), with potential antiangiogenic activity. Upon administration, tanibirumab specifically binds to VEGFR2, thereby preventing the binding of its ligand VEGF. This may result in the inhibition of tumor angiogenesis and a decrease in tumor nutrient supply. VEGFR2 is a pro-angiogenic growth factor receptor tyrosine kinase expressed by endothelial cells, while VEGF is overexpressed in many tumors and is correlated to tumor progression. PDQ Definition: A fully human monoclonal antibody targeting the vascular endothelial growth factor receptor 2 (VEGFR2), with potential antiangiogenic activity. Upon administration, tanibirumab specifically binds to VEGFR2, thereby preventing the binding of its ligand VEGF. This may result in the inhibition of tumor angiogenesis and a decrease in tumor nutrient supply. VEGFR2 is a pro-angiogenic growth factor receptor
    [Show full text]
  • Anatomy and Physiology of Peritoneal Dialysis
    Anatomy and Physiology of Peritoneal Dialysis Isaac Teitelbaum, MD Professor of Medicine Director, Acute & Home Dialysis Programs University of Colorado Hospital Denver, Colorado •1 Outline • Peritoneal cavity as a dialysis system • Models of peritoneal transport • Physiology of peritoneal transport Inverse relationship between solute transport and ultrafiltration • Kinetics of peritoneal transport • Synthesis & Application • Middle Molecules Anatomy of The Peritoneum • The lining of the abdominal cavity • Two layers: parietal - lines the anterior wall and undersurface of the diaphragm - 20% of total SA; blood supply from abdominal wall visceral - covers the abdominal organs - 80% of total SA; blood supply from mesenteric aa and portal vv Gokal R, Textbook of PD, pp. 61-70 •3 Anatomy of The Peritoneum • Size 1.5 – 2 m2; approximates BSA • Highly Vascular • Semi-permeable/bi-directional • “Lymphatic” drainage through diaphragmatic stomata • Continuous with Fallopian Tubes in females Gokal R, Textbook of PD, pp. 61-70 1. The two main properties of the peritoneal membrane are: a. Semi permeable – this allows substances of certain sizes to move from an area of greater concentration to less concentration. b. Bi Directional - substances move in either direction across the membrane. 2. So-called “lymphatic” drainage refers to bulk flow from the peritoneal cavity back to the circulation. This actually occurs across tissues as well as lymphatics. As this is convective flow, dissolved solutes move with the fluid. Thus, fluid reabsorption results in loss of solute clearance as well as loss of fluid removal. 3. It is important to be aware of the continuity of the peritoneal cavity with the Fallopian tubes as retrograde menstruation- which may occur in any woman but goes undetected- will cause bloody dialysate and create concern in the PD patient.
    [Show full text]
  • Comparison of Clinical Effects Between
    Kanno et al. Renal Replacement Therapy (2020) 6:7 https://doi.org/10.1186/s41100-019-0253-4 REVIEW Open Access Comparison of clinical effects between icodextrin and glucose solutions on outcomes of peritoneal dialysis: systematic review and meta-analysis of randomized controlled trials Atsuhiro Kanno1*, Yasushi Tsujimoto2, Takayuki Fujii3, Emi Fujikura4, Kimio Watanabe5, Hidemichi Yuasa6, Munekazu Ryuzaki7, Yasuhiko Ito8 and Hidetomo Nakamoto9 Abstract Background: Icodextrin enhances peritoneal filtration for patients on peritoneal dialysis (PD). However, clinically important outcomes have not yet been analyzed using authentic, objective statistical methods. The present systematic review aimed to determine the risks and benefits of icodextrin compared with a glucose-based solution with respect to clinically important and patient-centered outcomes. Methods: We systematically investigated only randomized controlled trials (RCTs) by adopting the Cochrane Database of Systematic Review (2014) and searched the CENTRAL, MEDLINE, and EMBASE databases for eligible studies reported in the literature. The quality of the evidence was assessed using the GRADE approach. Results: We finally evaluated important outcomes in 13 RCTs. Icodextrin significantly decreased the number of reported episodes of uncontrolled fluid overload in four RCTs that involved 236 patients (relative risk [RR], 0.31; 95% confidence interval [CI], 0.12 to 0.82; moderate certainty evidence). However, the inclusion of icodextrin for peritoneal ultrafiltration did not significantly differ in six RCTs involving 252 patients (mean difference [MD], 186.76 mL; 95% CI, − 47.08 to 420.59; low certainty evidence). Regarding other clinically important outcomes, all-cause mortality in 10 RCTs involving 1106 patients (RR, 0.75; 95% CI, 0.33 to 1.71; low certainty evidence) and technical survival in five RCTs involving 470 patients (RR, 0.57; 95%CI, 0.29 to 1.12; low certainty evidence) were not significant.
    [Show full text]
  • Malta Medicines List April 08
    Defined Daily Doses Pharmacological Dispensing Active Ingredients Trade Name Dosage strength Dosage form ATC Code Comments (WHO) Classification Class Glucobay 50 50mg Alpha Glucosidase Inhibitor - Blood Acarbose Tablet 300mg A10BF01 PoM Glucose Lowering Glucobay 100 100mg Medicine Rantudil® Forte 60mg Capsule hard Anti-inflammatory and Acemetacine 0.12g anti rheumatic, non M01AB11 PoM steroidal Rantudil® Retard 90mg Slow release capsule Carbonic Anhydrase Inhibitor - Acetazolamide Diamox 250mg Tablet 750mg S01EC01 PoM Antiglaucoma Preparation Parasympatho- Powder and solvent for solution for mimetic - Acetylcholine Chloride Miovisin® 10mg/ml Refer to PIL S01EB09 PoM eye irrigation Antiglaucoma Preparation Acetylcysteine 200mg/ml Concentrate for solution for Acetylcysteine 200mg/ml Refer to PIL Antidote PoM Injection injection V03AB23 Zovirax™ Suspension 200mg/5ml Oral suspension Aciclovir Medovir 200 200mg Tablet Virucid 200 Zovirax® 200mg Dispersible film-coated tablets 4g Antiviral J05AB01 PoM Zovirax® 800mg Aciclovir Medovir 800 800mg Tablet Aciclovir Virucid 800 Virucid 400 400mg Tablet Aciclovir Merck 250mg Powder for solution for inj Immunovir® Zovirax® Cream PoM PoM Numark Cold Sore Cream 5% w/w (5g/100g)Cream Refer to PIL Antiviral D06BB03 Vitasorb Cold Sore OTC Cream Medovir PoM Neotigason® 10mg Acitretin Capsule 35mg Retinoid - Antipsoriatic D05BB02 PoM Neotigason® 25mg Acrivastine Benadryl® Allergy Relief 8mg Capsule 24mg Antihistamine R06AX18 OTC Carbomix 81.3%w/w Granules for oral suspension Antidiarrhoeal and Activated Charcoal
    [Show full text]
  • Fluid and Pharmacological Agents for Adhesion Prevention After Gynaecological Surgery (Review)
    Fluid and pharmacological agents for adhesion prevention after gynaecological surgery (Review) Ahmad G, Mackie FL, Iles DA, O’Flynn H, Dias S, Metwally M, Watson A This is a reprint of a Cochrane review, prepared and maintained by The Cochrane Collaboration and published in The Cochrane Library 2014, Issue 7 http://www.thecochranelibrary.com Fluid and pharmacological agents for adhesion prevention after gynaecological surgery (Review) Copyright © 2014 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd. TABLE OF CONTENTS HEADER....................................... 1 ABSTRACT ...................................... 1 PLAINLANGUAGESUMMARY . 2 SUMMARY OF FINDINGS FOR THE MAIN COMPARISON . ..... 4 BACKGROUND .................................... 6 OBJECTIVES ..................................... 7 METHODS ...................................... 7 RESULTS....................................... 9 Figure1. ..................................... 10 Figure2. ..................................... 12 Figure3. ..................................... 13 Figure4. ..................................... 14 Figure5. ..................................... 15 Figure6. ..................................... 16 Figure7. ..................................... 17 Figure8. ..................................... 18 Figure9. ..................................... 18 Figure10. ..................................... 19 ADDITIONALSUMMARYOFFINDINGS . 22 DISCUSSION ..................................... 32 AUTHORS’CONCLUSIONS . 33 ACKNOWLEDGEMENTS . 33 REFERENCES ....................................
    [Show full text]
  • Country-Specific Glucose Monitor List
    Country-Specific Glucose Monitor List Country Name: USA Important Information This is a non-comprehensive list, current as of March 2015. Absence of a specific glucose monitor or test strips from this list does NOT imply compatibility or incompatibility with EXTRANEAL (Icodextrin) PD solution. Similarly, other glucose-measuring technologies which are not listed below (such as continuous glucose monitoring systems) may or may not be compatible with EXTRANEAL. Always contact the device manufacturer for current information. If the manufacturer cannot provide information regarding compatibility of the device with icodextrin and maltose, Baxter does NOT recommend that Extraneal patients use the product. Baxter reserves the right to change this list without notice and does not represent that it includes all potentially incompatible products. The glucose monitors manufacturers listed have certified to Baxter that they have tested (as per 2013 ISO 15197) their monitors with maltose and icodextrin to Baxter’s recommended limits: 278 mg/dL (maltose) and 1094 mg/dL (icodextrin). The manufacturers certified that their “green” monitors, below, showed no interference of blood glucose readings under these conditions, with the exception of the “green” monitors specifically notated6 for which certification of testing to Baxter’s recommended limits has not yet been received. This list is compiled from a search via: Internet, literature, Baxter internal studies, information from government agencies, test strip leaflets, safety alerts, and direct information from the product manufacturers. While efforts have been made to provide accurate and current information, Baxter does not manufacture these glucose monitors or test strips and thus does not guarantee the initial or continued accuracy of this information.
    [Show full text]
  • Marrakesh Agreement Establishing the World Trade Organization
    No. 31874 Multilateral Marrakesh Agreement establishing the World Trade Organ ization (with final act, annexes and protocol). Concluded at Marrakesh on 15 April 1994 Authentic texts: English, French and Spanish. Registered by the Director-General of the World Trade Organization, acting on behalf of the Parties, on 1 June 1995. Multilat ral Accord de Marrakech instituant l©Organisation mondiale du commerce (avec acte final, annexes et protocole). Conclu Marrakech le 15 avril 1994 Textes authentiques : anglais, français et espagnol. Enregistré par le Directeur général de l'Organisation mondiale du com merce, agissant au nom des Parties, le 1er juin 1995. Vol. 1867, 1-31874 4_________United Nations — Treaty Series • Nations Unies — Recueil des Traités 1995 Table of contents Table des matières Indice [Volume 1867] FINAL ACT EMBODYING THE RESULTS OF THE URUGUAY ROUND OF MULTILATERAL TRADE NEGOTIATIONS ACTE FINAL REPRENANT LES RESULTATS DES NEGOCIATIONS COMMERCIALES MULTILATERALES DU CYCLE D©URUGUAY ACTA FINAL EN QUE SE INCORPOR N LOS RESULTADOS DE LA RONDA URUGUAY DE NEGOCIACIONES COMERCIALES MULTILATERALES SIGNATURES - SIGNATURES - FIRMAS MINISTERIAL DECISIONS, DECLARATIONS AND UNDERSTANDING DECISIONS, DECLARATIONS ET MEMORANDUM D©ACCORD MINISTERIELS DECISIONES, DECLARACIONES Y ENTEND MIENTO MINISTERIALES MARRAKESH AGREEMENT ESTABLISHING THE WORLD TRADE ORGANIZATION ACCORD DE MARRAKECH INSTITUANT L©ORGANISATION MONDIALE DU COMMERCE ACUERDO DE MARRAKECH POR EL QUE SE ESTABLECE LA ORGANIZACI N MUND1AL DEL COMERCIO ANNEX 1 ANNEXE 1 ANEXO 1 ANNEX
    [Show full text]
  • (12) Patent Application Publication (10) Pub. No.: US 2006/0078604 A1 Kanios Et Al
    US 20060078604A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2006/0078604 A1 Kanios et al. (43) Pub. Date: Apr. 13, 2006 (54) TRANSDERMAL DRUG DELIVERY DEVICE Related U.S. Application Data INCLUDING AN OCCLUSIVE BACKING (60) Provisional application No. 60/616,861, filed on Oct. 8, 2004. (75) Inventors: David Kanios, Miami, FL (US); Juan A. Mantelle, Miami, FL (US); Viet Publication Classification Nguyen, Miami, FL (US) (51) Int. Cl. Correspondence Address: A 6LX 9/70 (2006.01) DCKSTEIN SHAPRO MORN & OSHINSKY (52) U.S. Cl. .............................................................. 424/449 LLP (57) ABSTRACT 2101 L Street, NW Washington, DC 20037 (US) A transdermal drug delivery system for the topical applica tion of one or more active agents contained in one or more (73) Assignee: Noven Pharmaceuticals, Inc. polymeric and/or adhesive carrier layers, proximate to a non-drug containing polymeric backing layer which can (21) Appl. No.: 11/245,180 control the delivery rate and profile of the transdermal drug delivery system by adjusting the moisture vapor transmis (22) Filed: Oct. 7, 2005 sion rate of the polymeric backing layer. Patent Application Publication Apr. 13, 2006 Sheet 1 of 2 US 2006/0078604 A1 Fis ZZZZZZZZZZZZZZZZZZZ :::::::::::::::::::::::::::::::: Patent Application Publication Apr. 13, 2006 Sheet 2 of 2 US 2006/0078604 A1 3. s s 3. a 3 : 8 g US 2006/0078604 A1 Apr. 13, 2006 TRANSIDERMAL DRUG DELVERY DEVICE 0008. In the “classic' reservoir-type device, the active INCLUDING AN OCCLUSIVE BACKING agent is typically dissolved or dispersed in a carrier to yield a non-finite carrier form, Such as, for example, a fluid or gel.
    [Show full text]
  • Queensland Health List of Approved Medicines
    Queensland Health List of Approved Medicines Drug Form Strength Restriction abacavir * For use in accord with PBS Section 100 indications * oral liquid See above 20 mg/mL See above tablet See above 300 mg See above abacavir + lamivudine * For use in accord with PBS Section 100 indications * tablet See above 600 mg + 300 mg See above abacavir + lamivudine + * For use in accord with PBS Section 100 indications * zidovudine tablet See above 300 mg + 150 mg + 300 mg See above abatacept injection 250 mg * For use in accord with PBS Section 100 indications * abciximab (a) Interventional Cardiologists for complex angioplasty (b) Interventional and Neuro-interventional Radiologists for rescue treatment of thromboembolic events that occur during neuroendovascular procedures. * Where a medicine is not TGA approved, patients should be made fully aware of the status of the medicine and appropriate consent obtained * injection See above 10 mg/5 mL See above abiraterone For use by medical oncologists as per the PBS indications for outpatient and discharge use only tablet See above 250 mg See above 500 mg See above acamprosate Drug and alcohol treatment physicians for use with a comprehensive treatment program for alcohol dependence with the goal of maintaining abstinence. enteric tablet See above 333 mg See above acarbose For non-insulin dependent diabetics with inadequate control despite diet; exercise and maximal tolerated doses of other anti-diabetic agents tablet See above 50 mg See above 100 mg See above acetazolamide injection 500 mg tablet 250 mg acetic acid ear drops 3% 15mL solution 2% 100mL green 3% 1 litre 6% 1 Litre 6% 200mL Generated on: 30-Aug-2021 Page 1 of 142 Drug Form Strength Restriction acetylcysteine injection For management of paracetamol overdose 2 g/10 mL See above 6 g/30 mL See above aciclovir cream Infectious disease physicians, haematologists and oncologists 5% See above eye ointment For use on the advice of Ophthalmologists only.
    [Show full text]
  • (12) Patent Application Publication (10) Pub. No.: US 2002/0102215 A1 100 Ol
    US 2002O102215A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2002/0102215 A1 Klaveness et al. (43) Pub. Date: Aug. 1, 2002 (54) DIAGNOSTIC/THERAPEUTICAGENTS (60) Provisional application No. 60/049.264, filed on Jun. 6, 1997. Provisional application No. 60/049,265, filed (75) Inventors: Jo Klaveness, Oslo (NO); Pal on Jun. 6, 1997. Provisional application No. 60/049, Rongved, Oslo (NO); Anders Hogset, 268, filed on Jun. 7, 1997. Oslo (NO); Helge Tolleshaug, Oslo (NO); Anne Naevestad, Oslo (NO); (30) Foreign Application Priority Data Halldis Hellebust, Oslo (NO); Lars Hoff, Oslo (NO); Alan Cuthbertson, Oct. 28, 1996 (GB)......................................... 9622.366.4 Oslo (NO); Dagfinn Lovhaug, Oslo Oct. 28, 1996 (GB). ... 96223672 (NO); Magne Solbakken, Oslo (NO) Oct. 28, 1996 (GB). 9622368.0 Jan. 15, 1997 (GB). ... 97OO699.3 Correspondence Address: Apr. 24, 1997 (GB). ... 9708265.5 BACON & THOMAS, PLLC Jun. 6, 1997 (GB). ... 9711842.6 4th Floor Jun. 6, 1997 (GB)......................................... 97.11846.7 625 Slaters Lane Alexandria, VA 22314-1176 (US) Publication Classification (73) Assignee: NYCOMED IMAGING AS (51) Int. Cl." .......................... A61K 49/00; A61K 48/00 (52) U.S. Cl. ............................................. 424/9.52; 514/44 (21) Appl. No.: 09/765,614 (22) Filed: Jan. 22, 2001 (57) ABSTRACT Related U.S. Application Data Targetable diagnostic and/or therapeutically active agents, (63) Continuation of application No. 08/960,054, filed on e.g. ultrasound contrast agents, having reporters comprising Oct. 29, 1997, now patented, which is a continuation gas-filled microbubbles stabilized by monolayers of film in-part of application No. 08/958,993, filed on Oct.
    [Show full text]
  • Pharmaceutical Compoundingand Dispensing, Second
    Pharmaceutical Compounding and Dispensing Pharmaceutical Compounding and Dispensing SECOND EDITION John F Marriott BSc, PhD, MRPharmS, FHEA Professor of Clinical Pharmacy Aston University School of Pharmacy, UK Keith A Wilson BSc, PhD, FRPharmS Head of School Aston University School of Pharmacy, UK Christopher A Langley BSc, PhD, MRPharmS, MRSC, FHEA Senior Lecturer in Pharmacy Practice Aston University School of Pharmacy, UK Dawn Belcher BPharm, MRPharmS, FHEA Teaching Fellow, Pharmacy Practice Aston University School of Pharmacy, UK Published by the Pharmaceutical Press 1 Lambeth High Street, London SE1 7JN, UK 1559 St Paul Avenue, Gurnee, IL 60031, USA Ó Pharmaceutical Press 2010 is a trade mark of Pharmaceutical Press Pharmaceutical Press is the publishing division of the Royal Pharmaceutical Society of Great Britain First edition published 2006 Second edition published 2010 Typeset by Thomson Digital, Noida, India Printed in Great Britain by TJ International, Padstow, Cornwall ISBN 978 0 85369 912 5 All rights reserved. No part of this publication may be reproduced, stored in a retrieval system, or transmitted in any form or by any means, without the prior written permission of the copyright holder. The publisher makes no representation, express or implied, with regard to the accuracy of the information contained in this book and cannot accept any legal responsibility or liability for any errors or omissions that may be made. The right of John F Marriott, Keith A Wilson, Christopher A Langley and Dawn Belcher to be identified as the author of this work has been asserted by them in accordance with the Copyright, Designs and Patents Act, 1988.
    [Show full text]